Reported Feb 8, 2023 · Ongoing
CADD Administration Set, List Numbers: a) REF 21-7346-24; b) REF 21-7363-24
Smiths Medical ASD Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Smiths Medical ASD Inc. · 6000 Nathan Ln N · Minneapolis, MN · 55442-1690
Is this the product you have?
- CADD Administration Set
- List Numbers
a) REF 21-7346-24b) REF 21-7363-24
- Lot codes and dates
- a) REF 21-7346-24UDI/DI 35019517161957
- Lot Numbers3776356 through 4320785
- b) REF 21-7363-24UDI/DI 3501951716196
- Lot Numbers3773412 through 4334343
- Amount recalled
- 1616714 units
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Stop using this product now
There are two potential issues with CADD Infusion System Infusion Sets: (1) Lack of Delivery or Underdelivery related to Tubing Occlusion and (2) False "No Disposable Attached (NDA)" Alarms
Using this product could cause serious injury, illness or death — stop using it now.
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